For researchers

Is your paper here?

2,673 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

15 matches for de Leeuw C.

Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Nature genetics · 2017 · PMID 28604731 · open access
12 pages+
rs72827839 rs62158211 rs61980273 rs182197129 rs543431433 rs553962214
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
rs9829032 rs10034259 rs200990 rs2194027 rs6490177 rs9516861
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs11646221 rs41293013 rs12479238 rs35731967 rs1248855 rs1486091
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Nature genetics · 2019 · PMID 30617256
12 pages+
rs10948363 rs9653111 rs183321458 rs539159088 rs11763230 rs28399637
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs2469933 rs1727284 rs442467 rs11135030 rs11210887 rs12053870
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
rs17223714 rs12534945 rs224029 rs11677484 rs4767645 rs12411886
The genetic architecture of human cortical folding
Science advances · 2021 · PMID 34910505 · open access
12 pages+
rs4143165 rs4732409 rs9874437 rs16831065 rs2468964 rs13390751
The Genetic Architecture of the Human Corpus Callosum and its Subregions
Nature communications · 2025 · PMID 41188267 · open access
12 pages+
rs113722141 rs71321439 rs4831182 rs6730884 rs2994330 rs686664
Multiscale analysis and functional validation of the cellular and genetic determinants of skeletal disease
International Federation of Musculoskeletal Research Societies (IFMRS) Big Data Working Group
Nature genetics · 2026 · PMID 42432248 · open access
12 pages+
rs5933080 rs8052826 rs11079173 rs33949355 rs1171561 rs60507951
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium and 1 more consortia
Nature genetics · 2013 · PMID 23974872 · open access
10 pages
rs114002140 rs7085104 rs6461049 rs1006737 rs17691888 rs17504622
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs10896090 rs10035291 rs111444407 rs10950456 rs57957974 rs17183814
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
rs1487441 rs9858213 rs13401104 rs3789044
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health
Communications biology · 2022 · PMID 35842455 · open access
2 pages
rs1160248 rs4301837

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.